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17 months ago
DareDevil
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4.3k
Exome sequencing is done at 100x coverage. Germline variants were called using GATK-HaplotypeCaller. When I looked at the VCF files, there are few variants showing higher depth than 100x. Some depth (DP) are like 120, 146, 153 etc
100x coverage is an average for the exome. Individual loci will vary. Did you try calculating the coverage yourself to see how it varies? Or perhaps examine various loci in a browser to see how it varies? If you look at the depth of all your variants from GATK, do you see a distribution of numbers? (i.e. some higher than 100x, some lower?)